Cyclopentaphenanthrene-based compound and organic electroluminescent device using the same

ABSTRACT

Provided are a cyclopentaphenanthrene-based compound and an organic EL device using the same. The cyclopentaphenanthrene-based compound is easy to prepare and excellent in solubility, color purity, and color stability. The cyclopentaphenanthrene-based compound is useful as a material for forming an organic layer, in particular, a light-emitting layer in an organic EL device, and as an organic dye or an electronic material such as a nonlinear optical material.

CROSS-REFERENCE TO RELATED PATENT APPLICATION AND CLAIM OF PRIORITY

This application claims priority from Korean Patent Application Nos.10-2006-0053900, filed on Jun. 15, 2006 and 10-2006-0113901,filed onNov. 17, 2006, in the Korean Intellectual Property Office, thedisclosure of which is incorporated herein in its entirety by reference.Furthermore, this application is a divisional of Applicants' U.S. Pat.No. 7,781,579 issued on the 24 of Aug. 2010, Ser. No. 11/812,260 filedin the U.S. Patent & Trademark Office on 15 Jun. 2007, and assigned tothe assignee of the present invention.

BACKGROUND OF THE INVENTION

1. Field of the Invention

The present invention relates to a cyclopentaphenanthrene-based compoundand to an organic electroluminescent device using the same. Moreparticularly, the present invention relates to acyclopentaphenanthrene-based compound and to an organicelectroluminescent device including an organic layer made of thecyclopentaphenanthrene-based compound.

2. Description of the Related Art

Organic electroluminescent (EL) devices (also referred to as organiclight-emitting devices) are active emission display devices that emitlight by recombination of electrons and holes in a thin layer(hereinafter, referred to as “organic layer”) made of a fluorescent orphosphorescent organic compound when a current is applied to the organiclayer. The organic EL devices have advantages such as lightweight,simple constitutional elements, easy fabrication process, superior imagequality, and wide viewing angle. In addition, the organic EL devices canperfectly create dynamic images, achieve high color purity, and haveelectrical properties suitable for portable electronic equipment due tolow power consumption and low driving voltage.

Eastman Kodak Co. developed an organic EL device of a multi-layeredstructure using an aluminum quinolinol complex layer and atriphenylamine derivative layer (U.S. Pat. No. 4,885,211), and anorganic EL device including an organic light-emitting layer made of alow molecular weight material capable of covering a broad emissionwavelength range from UV to visible light (U.S. Pat. No. 5,151,629).

Light-emitting devices are self-emission devices and have advantages ofa wide viewing angle, good contrast, and rapid response speed. Thelight-emitting devices can be classified into inorganic light-emittingdevices including a light-emitting layer made of an inorganic compoundand organic light-emitting devices (OLEDs; also referred to as “organicelectroluminescent devices” (organic EL devices)) including alight-emitting layer made of an organic compound. The OLEDs show betterbrightness, driving voltage, and response speed characteristics and canachieve polychromatic changes, compared to inorganic light-emittingdevices, and thus there have been many researches about OLEDs.

Generally, OLEDs have a stacked structure of an anode, an organiclight-emitting layer, and a cathode. OLEDs may also have variousstructures such as anode/hole injection layer/hole transportlayer/light-emitting layer/electron transport layer/electron injectionlayer/cathode or anode/hole injection layer/hole transportlayer/light-emitting layer/hole blocking layer/electron transportlayer/electron injection layer/cathode.

A material used in OLEDs can be divided into a vacuum depositionmaterial and a solution coating material according to a method offorming an organic layer. The vacuum deposition material must have avapor pressure of 10⁻⁶ torr or more at 500° C. or less, and may be a lowmolecular weight material with a molecular weight of 1200 or less. Thesolution coating material must have high solubility in a solvent toprepare a solution, and mainly includes an aromatic or heterocycliccompound.

In the case of manufacturing an OLED using a vacuum deposition process,manufacturing costs increase due to the use of a vacuum system. In thecase of using a shadow mask to form pixels for a natural color display,it is difficult to obtain high resolution pixels. On the other hand, inthe case of manufacturing an OLED using a solution coating process suchas inkjet printing, screen printing, or spin coating, manufacturing iseasy, manufacturing costs are low, and a relatively good resolution canbe achieved as compared to the case of using a shadow mask.

However, thermal stability, color purity, etc. of light-emittingmolecules of materials that can be used in the solution coating processare inferior to those that can be used in the vacuum deposition process.Even when the light-emitting molecules of the materials that can be usedin the solution coating process are excellent in thermal stability,color purity, etc., the materials may be crystallized to grow a crystalsize corresponding to a visible light wavelength range after they aremade into an organic layer, thereby scattering visible light, resultingin turbidity phenomenon, and pin holes may be formed, thereby causingdevice degradation.

Japanese Patent Laid-Open Publication No. 1999-003782 discloses ananthracene compound substituted by two naphthyl groups which can be usedin a light-emitting layer or a hole injection layer. However, theanthracene compound has poor solubility in a solvent, and an OLED usingthe compound exhibits unsatisfactory characteristics.

Therefore, there is still need to develop an organic EL device havingimproved driving voltage, brightness, efficiency and color purity, andgood thermal stability.

SUMMARY OF THE INVENTION

The present invention provides a compound and an organicelectroluminescent device using the compound.

The present invention provides a cyclopentaphenanthrene-based compoundwhich is available for both dry and wet processes, and has good thermalstability, emission characteristics and charge transport, and an organicEL device using the same.

According to an aspect of the present invention, there is provided acyclopentaphenanthrene-based compound represented by Formula 1 below:

wherein Y and Q are the same or different and each is a substituted orunsubstituted C2-C30 alkylene group, a substituted or unsubstitutedC6-C30 cycloalkylene group, a substituted or unsubstituted C6-C30arylene group, a substituted or unsubstituted C2-C30 heteroarylenegroup, or a substituted or unsubstituted C2-C30 alkenylene group;

m is an integer of 0 to 5;

n is an integer of 0 to 5;

R₁ and R₂ are the same or different and each is a hydrogen, a halogen, acyano group, a hydroxyl group, a substituted or unsubstituted C1-C20alkyl group, a substituted or unsubstituted C3-C20 cycloalkyl group, asubstituted or unsubstituted C2-C30 heterocycloalkyl group, asubstituted or unsubstituted C1-C20 alkoxy group, a substituted orunsubstituted C6-C30 aryl group, a substituted or unsubstituted C6-C30aralkyl group, a substituted or unsubstituted C2-C30 heteroaryl group,R₁ and R₂ may be linked together, and R₁ and R₂, when linked together,form a substituted or unsubstituted C3-C20 aliphatic ring, a substitutedor unsubstituted C5-C30 heteroaliphatic ring, a substituted orunsubstituted C6-C30 aromatic ring, or a substituted or unsubstitutedC2-C30 heteroaromatic ring;

R₃, R₄, R₅, R₆, R₇, and R₈ are the same or different and each is ahydrogen, a halogen, a cyano group, a hydroxyl group, a substituted orunsubstituted C1-C20 alkyl group, a substituted or unsubstituted C3-C20cycloalkyl group, a substituted or unsubstituted C2-C30 heterocycloalkylgroup, a substituted or unsubstituted C1-C20 alkoxy group, a substitutedor unsubstituted C6-C30 aryl group, a substituted or unsubstitutedC6-C30 aralkyl group, a substituted or unsubstituted C2-C30 heteroarylgroup, —N(G₁)(G₂), or —Si(G₃)(G₄)(G₅) where G₁, G₂, G₃, G₄, and G₅ areeach independently a hydrogen, a substituted or unsubstituted C1-C20alkyl group, a substituted or unsubstituted C6-C30 aryl group, asubstituted or unsubstituted C2-C30 heteroaryl group, a substituted orunsubstituted C5-C20 cycloalkyl group, or a substituted or unsubstitutedC2-C30 heterocycloalkyl group;

Z₁, Z₂, Z₃, and Z₄ are the same or different and each is a substitutedor unsubstituted C1-C20 alkyl group, a substituted or unsubstitutedC3-C20 cycloalkyl group, a substituted or unsubstituted C2-C30heterocycloalkyl group, a substituted or unsubstituted C1-C20 alkoxygroup, a substituted or unsubstituted C6-C30 aryl group, a substitutedor unsubstituted C2-C30 heteroaryl group, a substituted or unsubstitutedC6-C30 aralkyl group, a substituted or unsubstituted C8-C30 alkylarylgroup, a substituted or unsubstituted C1-C20 alkylene group, asubstituted or unsubstituted C6-C30 arylene group, or a substituted orunsubstituted C2-C30 heteroarylene group;

X is a single bond, —CH═CH—, —O—, —S—, —Se—, or —C(R′R″)— where R′ andR″ are the same as R₃, or —(CH₂)_(p)— where p is an integer of 1 to 10;and

o is 0 or 1.

R₁ and R₂ may be linked together to form one of rings represented byFormulae 2 through 5 below:

wherein “R₉”s are the same or different and each is a hydrogen, ahalogen, a cyano group, a hydroxyl group, a substituted or unsubstitutedC1-C20 alkyl group, a substituted or unsubstituted C3-C20 cycloalkylgroup, a substituted or unsubstituted C2-C30 heterocycloalkyl group, asubstituted or unsubstituted C1-C20 alkoxy group, a substituted orunsubstituted C6-C30 aryl group, a substituted or unsubstituted C6-C30aralkyl group, a substituted or unsubstituted C2-C30 heteroaryl group,—N(G₁)(G₂), or —Si(G₃)(G₄)(G₅) where G₁, G₂, G₃, G₄, and G₅ are eachindependently a hydrogen, a substituted or unsubstituted C1-C20 alkylgroup, a substituted or unsubstituted C6-C30 aryl group, a substitutedor unsubstituted C2-C30 heteroaryl group, a substituted or unsubstitutedC5-C20 cycloalkyl group, or a substituted or unsubstituted C2-C30heterocycloalkyl group; and

A is a single bond, —O—, —S—, —(CH₂)_(s)— where s is an integer of 1 to5.

According to an embodiment of the present invention, thecyclopentaphenanthrene-based compound of Formula 1 may be selected fromcompounds represented by Formulae 6 through 8 below:

wherein Y and Q are the same or different and each is a substituted orunsubstituted C2-C30 alkylene group, a substituted or unsubstitutedC6-C30 cycloalkylene group, a substituted or unsubstituted C6-C30arylene group, a substituted or unsubstituted C2-C30 heteroarylenegroup, or a substituted or unsubstituted C2-C30 alkenylene group;

m is an integer of 0 to 5;

n is an integer of 0 to 5;

R₁′ and R₂′ are the same or different and each is a hydrogen, a halogen,a cyano group, a hydroxyl group, a substituted or unsubstituted C1-C20alkyl group, a substituted or unsubstituted C3-C20 cycloalkyl group, asubstituted or unsubstituted C2-C30 heterocycloalkyl group, asubstituted or unsubstituted C1-C20 alkoxy group, a substituted orunsubstituted C6-C30 aryl group, a substituted or unsubstituted C6-C30aralkyl group, a substituted or unsubstituted C2-C30 heteroaryl group;

Z₁, Z₂, Z₃, and Z₄ are the same or different and each is a substitutedor unsubstituted C1-C20 alkyl group, a substituted or unsubstitutedC3-C20 cycloalkyl group, a substituted or unsubstituted C2-C30heterocycloalkyl group, a substituted or unsubstituted C1-C20 alkoxygroup, a substituted or unsubstituted C6-C30 aryl group, a substitutedor unsubstituted C2-C30 heteroaryl group, a substituted or unsubstitutedC6-C30 aralkyl group, a substituted or unsubstituted C2-C30 allylarylgroup, a substituted or unsubstituted C1-C20 alkylene group, asubstituted or unsubstituted C6-C30 arylene group, or a substituted orunsubstituted C2-C30 heteroarylene group;

X is a single bond, —CH═CH—, —O—, —S—, —Se—, or —C(R′R″)— where R′ andR″ are the same as R₃, or —(CH₂)_(p)— where p is an integer of 1 to 10;

o is 0 or 1; and

“R₁₀”s are the same or different and each is a hydrogen, a halogen, acyano group, a hydroxyl group, a substituted or unsubstituted C1-C20alkyl group, a substituted or unsubstituted C3-C20 cycloalkyl group, asubstituted or unsubstituted C2-C30 heterocycloalkyl group, asubstituted or unsubstituted C1-C20 alkoxy group, a substituted orunsubstituted C6-C30 aryl group, a substituted or unsubstituted C6-C30aralkyl group, a substituted or unsubstituted C2-C30 heteroaryl group,—N(G₁)(G₂), or —Si(G₃)(G₄)(G₅) where G₁, G₂, G₃, G₄, and G₅ are eachindependently a hydrogen, a substituted or unsubstituted C1-C20 alkylgroup, a substituted or unsubstituted C6-C30 aryl group, a substitutedor unsubstituted C2-C30 heteroaryl group, a substituted or unsubstitutedC5-C20 cycloalkyl group, or a substituted or unsubstituted C2-C30heterocycloalkyl group.

According to another aspect of the present invention, there is providedan organic EL device including: a first electrode; a second electrode;and at least one organic layer interposed between the first electrodeand the second electrode, the organic layer including theabove-described organic light-emitting compound.

BRIEF DESCRIPTION OF THE DRAWINGS

A more complete appreciation of the invention, and many of the attendantadvantages thereof, will be readily apparent as the same becomes betterunderstood by reference to the following detailed description whenconsidered in conjunction with the accompanying drawings in which likereference symbols indicate the same or similar components, wherein:

FIGS. 1A through 1C are schematic views illustrating organic EL devicesaccording to embodiments of the present invention; and

FIGS. 2A and 2B are graphs illustrating voltage-efficiencycharacteristics of organic EL devices according to embodiments of thepresent invention.

DETAILED DESCRIPTION OF THE INVENTION

The present invention will now be described more fully with reference tothe accompanying drawings, in which exemplary embodiments of theinvention are shown.

The present invention provides a cyclopentaphenanthrene-based compoundrepresented by Formula 1 below:

wherein Y and Q are the same or different and each is a substituted orunsubstituted C2-C30 alkylene group, a substituted or unsubstitutedC6-C30 cycloalkylene group, a substituted or unsubstituted C6-C30arylene group, a substituted or unsubstituted C2-C30 heteroarylenegroup, or a substituted or unsubstituted C2-C30 alkenylene group;

m is an integer of 0 to 5, preferably an integer of 0 to 2;

n is an integer of 0 to 5, preferably an integer of 0 to 2;

R₁ and R₂ are the same or different, and each is a hydrogen, a halogen,a cyano group, a hydroxyl group, a substituted or unsubstituted C1-C20alkyl group, a substituted or unsubstituted C3-C20 cycloalkyl group, asubstituted or unsubstituted C2-C30 heterocycloalkyl group, asubstituted or unsubstituted C1-C20 alkoxy group, a substituted orunsubstituted C6-C30 aryl group, a substituted or unsubstituted C6-C30aralkyl group, a substituted or unsubstituted C2-C30 heteroaryl group.R₁ and R₂ may be linked together, and R₁ and R₂, when linked together,form a substituted or unsubstituted C3-C20 aliphatic ring, a substitutedor unsubstituted C5-C30 heteroaliphatic ring, a substituted orunsubstituted C6-C30 aromatic ring, or a substituted or unsubstitutedC2-C30 heteroaromatic ring;

R₃, R₄, R₅, R₆, R₇, and R₈ are the same or different and each is ahydrogen, a halogen, a cyano group, a hydroxyl group, a substituted orunsubstituted C1-C20 alkyl group, a substituted or unsubstituted C3-C20cycloalkyl group, a substituted or unsubstituted C2-C30 heterocycloalkylgroup, a substituted or unsubstituted C1-C20 alkoxy group, a substitutedor unsubstituted C6-C30 aryl group, a substituted or unsubstitutedC6-C30 aralkyl group, a substituted or unsubstituted C2-C30 heteroarylgroup, —N(G₁)(G₂), or —Si(G₃)(G₄)(G₅) where G₁, G₂, G₃, G₄, and G₅ areeach independently a hydrogen, a substituted or unsubstituted C1-C20alkyl group, a substituted or unsubstituted C6-C30 aryl group, asubstituted or unsubstituted C2-C30 heteroaryl group, a substituted orunsubstituted C5-C20 cycloalkyl group, or a substituted or unsubstitutedC2-C30 heterocycloalkyl group;

Z₁, Z₂, Z₃, and Z₄ are the same or different and each is a substitutedor unsubstituted C1-C20 alkyl group, a substituted or unsubstitutedC3-C20 cycloalkyl group, a substituted or unsubstituted C2-C30heterocycloalkyl group, a substituted or unsubstituted C1-C20 alkoxygroup, a substituted or unsubstituted C6-C30 aryl group, a substitutedor unsubstituted C2-C30 heteroaryl group, a substituted or unsubstitutedC6-C30 aralkyl group, a substituted or unsubstituted C8-C30 allylarylgroup, a substituted or unsubstituted C1-C20 alkylene group, asubstituted or unsubstituted C6-C30 arylene group, or a substituted orunsubstituted C2-C30 heteroarylene group;

X is a single bond, —CH═CH—, —O—, —S—, —Se—, or —C(R′R″)— where R′ andR″ are the same as R₃, or —(CH₂)_(p)— where p is an integer of 1 to 10;and

o is 0 or 1.

When R₁ and R₂ are linked together, R₁ and R₂ preferably form onerepresented by Formulae 2 through 5 below:

wherein “R₉”s are the same or different and each is a hydrogen, ahalogen, a cyano group, a hydroxyl group, a substituted or unsubstitutedC1-C20 alkyl group, a substituted or unsubstituted C3-C20 cycloalkylgroup, a substituted or unsubstituted C2-C30 heterocycloalkyl group, asubstituted or unsubstituted C1-C20 alkoxy group, a substituted orunsubstituted C6-C30 aryl group, a substituted or unsubstituted C6-C30aralkyl group, a substituted or unsubstituted C2-C30 heteroaryl group,—N(G₁)(G₂), or —Si(G₃)(G₄)(G₅) where G₁, G₂, G₃, G₄, and G₅ are eachindependently a hydrogen, a substituted or unsubstituted C1-C20 alkylgroup, a substituted or unsubstituted C6-C30 aryl group, a substitutedor unsubstituted C2-C30 heteroaryl group, a substituted or unsubstitutedC5-C20 cycloalkyl group, or a substituted or unsubstituted C2-C30heterocycloalkyl group; and

A is a single bond, —O—, —S—, or —(CH₂)_(s)— where s is an integer of 1to 5.

In particular, in the compounds of Formulae 1-5, R₁ through R₉ serve toenhance film processibility by increasing the solubility and amorphousproperty of the compounds.

The compound of Formula 1 according to the present invention may beselected from compounds represented by Formulae 6 through 8 below:

wherein Y and Q are the same or different and each is a substituted orunsubstituted C2-C30 alkylene group, a substituted or unsubstitutedC6-C30 cycloalkylene group, a substituted or unsubstituted C6-C30arylene group, a substituted or unsubstituted C2-C30 heteroarylenegroup, or a substituted or unsubstituted C2-C30 alkenylene group;

m is an integer of 0 to 5, preferably an integer of 0 to 2;

n is an integer of 0 to 5, preferably an integer of 0 to 2;

R₁′ and R₂′ are the same or different and each is a hydrogen, a halogen,a cyano group, a hydroxyl group, a substituted or unsubstituted C1-C20alkyl group, a substituted or unsubstituted C3-C20 cycloalkyl group, asubstituted or unsubstituted C2-C30 heterocycloalkyl group, asubstituted or unsubstituted C1-C20 alkoxy group, a substituted orunsubstituted C6-C30 aryl group, a substituted or unsubstituted C6-C30aralkyl group, a substituted or unsubstituted C2-C30 heteroaryl group;

Z₁, Z₂, Z₃, and Z₄ are the same or different and each is a substitutedor unsubstituted C1-C20 alkyl group, a substituted or unsubstitutedC3-C20 cycloalkyl group, a substituted or unsubstituted C2-C30heterocycloalkyl group, a substituted or unsubstituted C1-C20 alkoxygroup, a substituted or unsubstituted C6-C30 aryl group, a substitutedor unsubstituted C2-C30 heteroaryl group, a substituted or unsubstitutedC6-C30 aralkyl group, a substituted or unsubstituted C2-C30 allylarylgroup, a substituted or unsubstituted C1-C20 alkylene group, asubstituted or unsubstituted C6-C30 arylene group, or a substituted orunsubstituted C2-C30 heteroarylene group;

X is a single bond, —CH═CH—, —O—, —S—, —Se—, or —C(R′R″)— where R′ andR″ are the same as R₃, or —(CH₂)_(p)— where p is an integer of 1 to 10;

o is 0 or 1; and

“R₁₀”s are the same or different and each is a hydrogen, a halogen, acyano group, a hydroxyl group, a substituted or unsubstituted C1-C20alkyl group, a substituted or unsubstituted C3-C20 cycloalkyl group, asubstituted or unsubstituted C2-C30 heterocycloalkyl group, asubstituted or unsubstituted C1-C20 alkoxy group, a substituted orunsubstituted C6-C30 aryl group, a substituted or unsubstituted C6-C30aralkyl group, a substituted or unsubstituted C2-C30 heteroaryl group,—N(G₁)(G₂), or —Si(G₃)(G₄)(G₅) where G₁, G₂, G₃, G₄, and G₅ are eachindependently a hydrogen, a substituted or unsubstituted C1-C20 alkylgroup, a substituted or unsubstituted C6-C30 aryl group, a substitutedor unsubstituted C2-C30 heteroaryl group, a substituted or unsubstitutedC5-C20 cycloalkyl group, or a substituted or unsubstituted C2-C30heterocycloalkyl group.

In the above formula, the “aryl group” refers to a monovalent grouphaving an aromatic ring system and may contain one, two or more ringsystems. The two or more ring systems may be attached to each other ormay be fused. The “heteroaryl group” refers to an aryl group in which atleast one carbon atom is substituted by at least one selected from thegroup consisting of N, O, S, and P.

The “cycloalkyl group” refers to an alkyl group having a ring system,and the “heterocycloalkyl group” refers to a cycloalkyl group in whichat least one carbon atom is substituted by at least one selected fromthe group consisting of N, O, S, and P.

In the above formula, the alkyl group, the alkoxy group, the aryl group,the heteroaryl group, the cycloalkyl group, and the heterocycloalkylgroup may be substituted by at least one substituent selected from thegroup consisting of —F; —Cl; —Br; —CN; —NO₂; —OH; a C1-C20 alkyl groupwhich is unsubstituted or substituted by —F, —Cl, —Br, —CN, —NO₂, or—OH; a C1-C20 alkoxy group which is unsubstituted or substituted by —F,—Cl, —Br, —CN, —NO₂, or —OH; a C6-C30 aryl group which is unsubstitutedor substituted by a C1-C20 alkyl group, a C1-C20 alkoxy group, —F, —Cl,—Br, —CN, —NO₂, or —OH; a C2-C30 heteroaryl group which is unsubstitutedor substituted by a C1-C20 alkyl group, a C1-C20 alkoxy group, —F, —Cl,—Br, —CN, —NO₂, or —OH; a C5-C20 cycloalkyl group which is unsubstitutedor substituted by a C1-C20 alkyl group, a C1-C20 alkoxy group, —F, —Cl,—Br, —CN, —NO₂, or —OH; a C2-C30 heterocycloalkyl group which isunsubstituted or substituted by a C1-C20 alkyl group, a C1-C20 alkoxygroup, —F, —Cl, —Br, —CN, —NO₂, or —OH; and —N(G₆)(G₇). At this time, G₆and G₇ are the same or different and each may be a hydrogen; a C1-C10alkyl group; or a C6-C30 aryl group substituted by a C1-C10 alkyl group.

In more detail, R₁-R₁₀ are the same or different and each may beselected from the group consisting of a hydrogen, a halogen, a cyanogroup, a hydroxyl group, a substituted or unsubstituted C1-C10 alkylgroup, a substituted or unsubstituted C1-C10 alkoxy group, and asubstituted or unsubstituted group as follows: a phenyl group, abiphenyl group, a pentalenyl group, an indenyl group, a naphthyl group,a biphenylenyl, an anthracenyl group, an azulenyl group, a heptalenylgroup, an acenaphthylenyl group, a phenalenyl group, a fluorenyl group,a methylanthryl group, a phenanthrenyl group, a triphenylenyl group, apyrenyl group, a chrysenyl group, an ethyl-chrysenyl group, a picenylgroup, a perylenyl group, a chloroperylenyl group, a pentaphenyl group,a pentacenyl group, a tetraphenylenyl group, a hexaphenyl group, ahexacenyl group, a rubicenyl group, a coronenyl group, a trinaphthylenylgroup, a heptaphenyl group, a heptacenyl group, a pyranthrenyl group, anovalenyl group, a carbazolyl group, a thiophenyl group, an indolylgroup, a purinyl group, a benzimidazolyl group, a quinolinyl group, abenzothiophenyl group, a parathiazinyl group, a pyrrolyl group, apyrazolyl group, an imidazolyl group, an imidazolinyl group, an oxazolylgroup, a thiazolyl group, a triazolyl group, a tetrazolyl group, anoxadiazolyl group, a pyridinyl group, a pyridazinyl group, a pyrimidinylgroup, a pyrazinyl group, a thianthrenyl group, a cyclopentyl group, acyclohexyl group, an oxiranyl group, a pyrrolidinyl group, apyrazolidinyl group, an imidazolidinyl group, a piperidinyl group, apiperazinyl group, a morpholinyl group, a di(C6-C30 aryl)amino group, atri(C6-C30 aryl)silyl group, or a derivative thereof.

The term “derivative(s)” refers to a compound derived or obtained fromanother and containing essential elements of the above-illustratedgroup(s). Preferably, the term “derivative(s)” refers to theabove-illustrated group(s) wherein at least one hydrogen is substitutedby a substituent as described above.

The cyclopentaphenanthrene-based compound of the present invention maybe selected from the group consisting of compounds represented byFormulae 9 through 46 below, but is not limited thereto:

The compound of Formula 1 according to the present invention can besynthesized using a common synthesis method. For a detailed synthesismethod of the compound of the present invention, reference will be madeto the reaction schemes in the following synthesis examples.

The present invention also provides an organic EL device including:

a first electrode;

a second electrode; and

an organic layer interposed between the first electrode and the secondelectrode, the organic layer including at least one compound representedby Formula 1 above.

The compound of Formula 1 above is suitable for an organic layer of anorganic EL device, in particular, a light-emitting layer (also referredto as an emissive layer), a hole injection layer, or a hole transportlayer.

An organic EL device according to the present invention includes acompound which has good solubility and thermal stability and can form astable organic layer, and thus, can provide a good driving voltage andenhanced emission characteristics (e.g., color purity), unlike aconventional organic EL device including a less stable organic layerwhen manufactured using a solution coating process.

The organic EL device according to the present invention can bevariously structured. That is, the organic EL device may further includeat least one layer selected from the group consisting of a holeinjection layer, a hole transport layer, a hole blocking layer, anelectron blocking layer, an electron transport layer, and an electroninjection layer, between the first electrode and the second electrode.

In more detail, embodiments of the organic EL device according to thepresent invention are illustrated in FIGS. 1A, 1B, and 10. Referring toFIG. 1A, an organic EL device has a stacked structure of firstelectrode/hole injection layer/hole transport layer/light-emittinglayer/electron transport layer/electron injection layer/secondelectrode. Referring to FIG. 1B, an organic EL device has a stackedstructure of first electrode/hole injection layer/light-emittinglayer/electron transport layer/electron injection layer/secondelectrode. Referring to FIG. 10, an organic EL device has a stackedstructure of first electrode/hole injection layer/hole transportlayer/light-emitting layer/hole blocking layer/electron transportlayer/electron injection layer/second electrode. At this time, at leastone of the light-emitting layer, the hole injection layer, and the holetransport layer may include the compound of Formula 1 of the presentinvention.

A light-emitting layer of the organic EL device according to the presentinvention may include a red, green, blue, or white phosphorescent orfluorescent dopant. The phosphorescent dopant may be an organometalliccompound including at least one element selected from the groupconsisting of Ir, Pt, Os, Ti, Zr, Hf, Eu, Tb, and Tm.

Hereinafter, a method of manufacturing an organic EL device according tothe present invention will be described with reference to FIG. 1C.

First, a first electrode material with a high work function is formed ona substrate using deposition or sputtering to form a first electrode.The first electrode may be an anode. Here, the substrate may be asubstrate commonly used in organic EL devices. Preferably, the substratemay be a glass substrate or a transparent plastic substrate which isexcellent in mechanical strength, thermal stability, transparency,surface smoothness, handling property, and water repellency. The firstelectrode material may be a material with good transparency andconductivity, e.g., indium tin oxide (ITO), indium zinc oxide (IZO), tinoxide (SnO₂), or zinc oxide (ZnO).

Next, a hole injection layer (HIL) may be formed on the first electrodeusing various methods such as vacuum deposition, spin-coating, casting,or Langmuir-Blodgett (LB) method.

In the case of forming the hole injection layer using a vacuumdeposition process, the deposition conditions vary according to the typeof a hole injection layer material, the structure and thermalcharacteristics of the hole injection layer, etc. However, it ispreferred that the hole injection layer is deposited to a thickness of10 Å to 5 μm at a deposition rate of 0.01 to 100 Å/sec, at a temperatureof 100 to 500° C., in a vacuum level of 10⁻⁸ to 10⁻³ torr.

In the case of forming the hole injection layer using a spin-coatingprocess, the coating conditions vary according to the type of a holeinjection layer material, the structure and thermal characteristics ofthe hole injection layer, etc. However, it is preferred that thespin-coating is performed at a coating speed of about 2000 to 5000 rpm,and, after the spin-coating, a thermal treatment is performed at atemperature of about 80 to 200° C. for the purpose of solvent removal.

The hole injection layer material may be a compound of Formula 1 asdescribed above. In addition, the hole injection layer material may be aknown hole injection material, e.g., a phthalocyanine compound (e.g.,copper phthalocyanine) disclosed in U.S. Pat. No. 4,356,429, aStarburst-type amine derivative (e.g., TCTA, m-MTDATA, or m-MTDAPB)disclosed in Advanced Material, 6, p. 677 (1994), or a solubleconductive polymer, e.g., Pani/DBSA (Polyaniline/Dodecylbenzenesulfonicacid), PEDOT/PSS(Poly(3,4-ethylenedioxythiophene)/Poly(4-styrenesulfonate)), Pani/CSA(Polyaniline/Camphor sulfonic acid), or PANI/PSS(Polyaniline)/Poly(4-styrenesulfonate).

The hole injection layer may be formed to a thickness of about 100 to10,000 Å, preferably 100 to 1,000 Å. If the thickness of the holeinjection layer is less than 100 Å, hole injection characteristics maybe lowered. On the other hand, if the thickness of the hole injectionlayer exceeds 10,000 Å, a driving voltage may be increased.

Next, a hole transport layer (HTL) may be formed on the hole injectionlayer using various methods such as vacuum deposition, spin-coating,casting, or LB method. In the case of forming the hole transport layerusing vacuum deposition or spin-coating, the deposition or coatingconditions vary according to the type of a used compound, but aregenerally almost the same as those for the formation of the holeinjection layer.

A hole transport layer material may be a compound of Formula 1 asdescribed above. In addition, the hole transport layer material can be aknown hole transport material, e.g., a carbazole derivative such asN-phenylcarbazole or polyvinylcarbazole; an amine derivative having anaromatic fused ring system such asN,N′-bis(3-methylphenyl)-N,N′-diphenyl-[1,1-biphenyl]-4,4′-diamine (TPD)or N,N′-di(naphthalene-1-yl)-N,N′-diphenylbenzidine (α-NPD), etc.

The hole transport layer may be formed to a thickness of about 50 to1,000 Å, preferably 100 to 600 Å. If the thickness of the hole transportlayer is less than 50 Å, hole transport characteristics may be lowered.On the other hand, if the thickness of the hole transport layer exceeds1,000 Å, a driving voltage may be increased.

Next, a light-emitting layer (EML) is formed on the hole transport layerusing vacuum deposition, spin-coating, casting, or LB method. In thecase of forming the light-emitting layer using vacuum deposition orspin-coating, the deposition or coating conditions vary according to thetype of a used compound, but are generally almost the same as those forthe formation of the hole injection layer.

The light-emitting layer may include a compound of Formula 1 asdescribed above. At this time, a known fluorescent host material or aknown dopant material suitable for the compound of Formula 1 may also beused. The compound of Formula 1 can be used as a phosphorescent hostalone or in combination with CBP (4,4′-N,N′-dicarbazole-biphenyl), PVK(poly(n-vinylcarbazole)), etc. A red phosphorescent dopant (e.g., PtOEP,RD 61 (UDC)), a green phosphorescent dopant (e.g., Ir(PPy)₃(PPy=2-phenylpyridine)), or a blue phosphorescent dopant (e.g., F₂Irpic)may be used as a phosphorescent dopant.

When the compound of Formula 1 is used as a dopant, the dopingconcentration of the dopant is not particularly limited. Generally, thecontent of the dopant is 0.01 to 15 parts by weight based on 100 partsby weight of a host. When the compound of Formula 1 is used as a singlehost, the doping concentration of a dopant is not particularly limited.Generally, the content of a dopant is 0.01 to 15 parts by weight basedon 100 parts by weight of the host. When the compound of Formula 1 isused as a host in combination with another host, the content of thecompound of Formula 1 is 30-99 parts by weight based on the total weight(100 parts by weight) of the hosts.

The light-emitting layer may be formed to a thickness of about 100 to1,000 Å, preferably 200 to 600 Å. If the thickness of the light-emittinglayer is less than 100 Å, emission characteristics may be lowered. Onthe other hand, if the thickness of the light-emitting layer exceeds1,000 Å, a driving voltage may be increased.

In a case where the light-emitting layer includes a phosphorescentdopant, a hole blocking layer (HBL) may be formed on the hole transportlayer using vacuum deposition, spin-coating, casting, or LB method, inorder to prevent the diffusion of triplet excitons or holes into anelectron transport layer. In the case of forming the hole blocking layerusing vacuum deposition or spin coating, the deposition or coatingconditions vary according to the type of a used compound, but aregenerally almost the same as those for the formation of the holeinjection layer. An available hole blocking material may be anoxadiazole derivative, a triazole derivative, a phenanthrolinederivative, BCP, an aluminum complex, etc.

The hole blocking layer may be formed to a thickness of about 50 to1,000 Å, preferably 100 to 300 Å. If the thickness of the hole blockinglayer is less than 50 Å, hole blocking characteristics may be lowered.On the other hand, if the thickness of the hole blocking layer exceeds1,000 Å, a driving voltage may be increased.

Next, an electron transport layer (ETL) may be formed using variousmethods such as vacuum deposition, spin-coating, or casting. In the caseof forming the electron transport layer using vacuum deposition orspin-coating, the deposition or coating conditions vary according to thetype of a used compound, but are generally almost the same as those forthe formation of the hole injection layer. An electron transport layermaterial serves to stably transport electrons from an electron donorelectrode (a cathode) and may be a known material such as anoxazole-based compound, an isoxazole-based compound, a triazole-basedcompound, an isothiazole-based compound, an oxadiazole-based compound, athiadiazole-based compound, a perylene-based compound, an aluminumcomplex (e.g.: Alq3 (tris(8-quinolinolato)-aluminum) BAlq, SAlq, orAlmq3), a gallium complex (e.g.: Gaq′2OPiv, Gaq′2OAc, 2(Gaq′2)), etc.

The electron transport layer may be formed to a thickness of about 100to 1,000 Å, preferably 200 to 500 Å. If the thickness of the electrontransport layer is less than 100 Å, electron transport characteristicsmay be lowered. On the other hand, if the thickness of the electrontransport layer exceeds 1,000 Å, a driving voltage may be increased.

An electron injection layer (EIL) may be formed on the electrontransport layer in order to facilitate the injection of electrons from acathode into the light-emitting layer. An electron injection layermaterial is not particularly limited.

The electron injection layer material may be optionally selected fromknown materials such as LiF, NaCl, CsF, Li₂O, or BaO. The depositionconditions of the electron injection layer vary according to the type ofa used compound, but are generally almost the same as those for theformation of the hole injection layer.

The electron injection layer may be formed to a thickness of about 1 to100 Å, preferably 5 to 50 Å. If the thickness of the electron injectionlayer is less than 1 Å, electron injection characteristics may belowered. On the other hand, if the thickness of the electron injectionlayer exceeds 100 Å, a driving voltage may be increased.

Finally, a second electrode is formed on the electron injection layerusing vacuum deposition or sputtering. The second electrode may be usedas a cathode. A material for forming the second electrode may be metalor alloy with a low work function, an electroconductive compound, or amixture thereof. For example, the second electrode forming material maybe lithium (Li), magnesium (Mg), aluminum (Al), aluminum-lithium(Al—Li), calcium (Ca), magnesium-indium (Mg—In), magnesium-silver(Mg—Ag), etc. The second electrode may also be a transmissive cathodemade of ITO or IZO to provide a front-emission type device.

Hereinafter, the present invention will be described more specificallywith reference to the following working examples. However, the followingexamples are for illustrative purposes and are not intended to limit thescope of the invention.

EXAMPLES

Synthesis Example 1 1) Synthesis of8,9-dihydro-4H-cyclopenta[def]phenanthrene

4H-cyclopenta[def]phenanthrene (4.75 g, 25 mmol) was placed in a Parreactor bottle, and EtOH (200 ml) was added thereto. 5% Pd/C (3.99 g)was added to the reaction solution, and the resultant solution wasincubated under a hydrogen pressure of 40 psi for 24 hours. After thereaction was terminated, the reaction solution was filtered, and thefiltrate was concentrated under a reduced pressure to give a whiteproduct (4.42 g, 90%).

¹H NMR (300 MHz, CDCl₃, δ): 7.36(2H, d), 7.21(2H, t), 7.12(2H, d),3.90(2H, s), 3.16 (4H, s)

2) Synthesis of 2,6-dibromo-8,9-dihydro-4H-cyclopenta[def]phenanthrene

8,9-dihydro-4H-cyclopenta[def]phenanthrene (4.42 g, 23 mmol) was placedin a 250 ml round bottom flask (RBF), and CCl₄ (100 ml) was addedthereto. The reaction mixture was cooled to 0° C., and Br₂ (7.72 g, 48mmol) was dropwise added thereto. The reaction solution was incubatedfor 4 hours and a 10% NaSO₃ solution was added thereto. The organiclayer was separated, concentrated under a reduced pressure, andrecrystallized from n-hexane to give a titled compound (4.45 g, 55%).

¹H NMR (300 MHz, CDCl₃, δ): 7.48(2H, s), 7.28(2H, s), 3.85(2H, s),3.10(4H, s)

3) Synthesis of Compound 1

2,6-dibromo-8,9-dihydro-4H-cyclopenta[def]phenanthrene (4.45 g, 12.7mmol) in a 250 ml round bottom flask was dissolved with xylene, ando-chloranil (4.15 g) was added thereto at room temperature. The reactionmixture was heated and refluxed in an oil bath for 72 hours. After thereaction was terminated, the reaction solution was cooled andconcentrated under a reduced pressure. The residue was purified bysilica gel column chromatography (mobile solvent: n-hexane) to give acompound 1 (3.6 g, 81%).

¹H NMR (300 MHz, CDCl₃, δ): 7.98(2H, s), 7.79(2H, s), 7.73(2H, s),4.28(2H, s)

4) Synthesis of Compound 2

2,6-dibromo-4H-cyclopenta[def]phenanthrene (2.6 g, 7.7 mmol), t-BuOK(20.8 g, 61.6 mmol), DMSO (20 ml), and HMPA (20 ml) was placed in 50 mlround bottom flask with a syringe. The mixture was stirred for 50minutes at room temperature and cooled to 0° C. CH₃l (3.75 ml, 61.6mmol) was dropped to the mixture with a syringe and the resultantsolution was stirred for 30 minutes at 0° C. Then, water (50 ml) andmethylene chloride (50 ml) were added to the solution to separate anorganic layer. The organic layer was purified by silica gel columnchromatography to obtain compound 2 (3.6 g, 80%). ¹H NMR (300 MHz,CDCl₃, δ): 7.98(2H, s), 7.79(2H, s), 7.73(2H, s), 1.93(m, 6H).

5) Synthesis of Material 1 (Formula 9)

The compound 2 (0.65 g, 1.747 mmol), bis(4-biphenyl)amine (TCI Corp.)(1.40 g, 4.37 mmol), sodium tert-butoxide (0.51 g, 0.5 mmol), Pd₂(dba)₃[(tris(dibenzylidene acetone) dipalladium(0))] (0.08 g, 0.087 mmol), andtri(tert-butyl)phosphine (0.017 g, 0.087 mmol) in a 50 ml round bottomflask were dissolved with toluene (10 mL), and the reaction mixture wasrefluxed for 12 hours. After the reaction was terminated, the reactionsolution was cooled to room temperature and extracted with distilledwater (100 ml). The combined organic layers were dried over MgSO₄,concentrated, and purified by silica gel column chromatography. Theeluate was concentrated and dried to give a material 1 represented byFormula 9 (1.1 g, yield: 75%).

¹H NMR (300 MHz, CDCl₃, δ):7.90(2H, s), 7.75(2H, s), 7.72(2H, s),7.48-6.62 (m, 36H), 1.92(m, 6H).

Synthesis Example 2 1) Synthesis of Compound 3

2,6-dibromo-4H-cyclopenta[def]phenanthrene (2.6 g, 7.7 mmol) and octylbromide (3.6 g, 18.5 mmol) in a 50 ml round bottom flask were dissolvedwith toluene (10 ml), and TBAB (tetrabutylammoniumbromide) (0.125 g,0.385 mmol) was added thereto. A solution of NaOH (3.1 g, 77 mmol) inwater (50 ml) was added to the reaction mixture, and the resultantsolution was refluxed for two days. After the reaction was terminated,the reaction solution was extracted with chloroform. The organic layerwas dried over MgSO₄, concentrated, and purified by silica gel columnchromatography (eluent: n-hexane). The eluate was distilled under areduced pressure to remove unreacted octyl bromide, thereby giving acompound 2 (3.6 g, 80%).

¹H NMR (300 MHz, CDCl₃, δ): 7.98(2H, s), 7.79(2H, s), 7.73(2H, s),1.93(m, 4H), 1.21(m, 20H), 0.87(m, 6H), 0.65(broad s, 4H)

2) Synthesis of Material 2 (Formula 10)

The compound 2 (1 g, 1.747 mmol), diphenylamine (0.88 g, 5.241 mmol),sodium tert-butoxide (0.51 g, 0.5 mmol), Pd₂(dba)₃ [(tris(dibenzylideneacetone) dipalladium(0))] (0.08 g, 0.087 mmol), andtri(tert-butyl)phosphine (0.017 g, 0.087 mmol) in a 50 ml round bottomflask were dissolved with toluene (10 mL), and the reaction mixture wasrefluxed for 12 hours. After the reaction was terminated, the reactionsolution was cooled to a room temperature and extracted with distilledwater (100 ml). The combined organic layers were dried over MgSO₄,concentrated, and purified by silica gel column chromatography. Theeluate was concentrated and dried to give a material 1 represented byFormula 9 (10.9 g, yield: 70%).

¹H NMR (300 MHz, CDCl₃, δ): 7.98-6.74 (m, 26H), 1.93(m, 4H), 1.21(m,20H), 0.87(m, 6H), 0.65(broad s, 4H).

Synthesis Example 3 1) Synthesis of2,6-dibromo-cyclopenta[def]phenanthren-4-one

Benzene (200 ml) was placed in a 250 ml round bottom flask, and thecompound 1 (3.6 g, 10.4 mmol) was added thereto. MnO₂ (150 g) was addedto the reaction mixture, and the resultant mixture was heated andrefluxed in an oil bath for 18 hours. After the reaction was terminated,the reaction solution was filtered to remove MnO₂, and sufficientlywashed with CHCl₃, THF, and MeOH in sequence. The filtrate wasconcentrated under a reduced pressure and the residue was recrystallizedfrom acetone to give the titled compound (1.45 g, 39%).

¹H NMR (300 MHz, CDCl₃, δ): 8.08(2H, s), 7.89(2H, s), 7.74(2H, s)

2) Synthesis of Intermediate A

2-bromobiphenyl (0.68 g, 2.95 mmol) was dissolved in anhydrous THF (10ml), and the reaction mixture was cooled to −78° C. Then, t-BuLi (3.5ml) was gradually dropwise added. The reaction mixture was stirred forone hour, and a solution of 2,6-dibromo-cyclopenta[def]phenanthren-4-one(1 g, 2.95 mmol) in anhydrous THF (5 ml) was dropwise added thereto for30 minutes. After the reaction was terminated, the reaction solution wasconcentrated under a reduced pressure and extracted with ethylacetateand brine to separate an organic layer. The organic layer wasconcentrated and the residue was purified by silica gel columnchromatography to give an intermediate A (3.6 g).

3) Synthesis of Compound 4

The intermediate A was dissolved in acetic acid (30 ml), and thereaction solution was cooled to 0° C. Then, HCl (1 ml) was dropwiseadded and the reaction mixture was incubated for two hours. After thereaction was terminated, the reaction solution was filtered and washedwith acetic acid and methanol to give a white solid (2 g, 80%).

4) Synthesis of Material 3 (Formula 13)

A material 3 represented by Formula 13 was synthesized in the samemanner as in the synthesis of the material 1 of Synthesis Example 1except that the compound 4 was used instead of the compound 2 and9H-carbazole was used instead of Bis(4-biphenyl)amine.

¹H NMR (300 MHz, CDCl₃, δ): 8.10-6.82 (m, 30H)

5) Synthesis of Material 4 (Formula 14)

The compound 4 (1 g, 1.747 mmol),di-naphthalene-2-yl-[4-(4,4,5,5-tetramethyl-[1,3,2]dioxabororane-2-yl)-phenyl]-amine(1.81 g, 3.843 mmol), K₂CO₃ (1.935 g, 0.014 mmol),tetrakis(triphenylphosphine)palladium (0) (0.4 g, 0.35 mmol), andtetrabutylammoniumbromide (1.13 g, 3.49 mmol) in a 50 ml round bottomflask were dissolved with toluene (10 ml) and THF (10 ml), and thereaction mixture was refluxed for 12 hours. After the reaction wasterminated, the reaction solution was cooled to a room temperature andextracted with distilled water (100 ml) to separate an organic layer.The combined organic layers were dried over MgSO₄, concentrated, andpurified by silica gel column chromatography. The eluate wasconcentrated and dried to give a material 4 represented by Formula 14(0.8 g, yield: 45%).

¹H NMR (300 MHz, CDCl₃, δ): 8.15-6.54 (m, 50H)

Synthesis Example 4 1) Synthesis of Intermediate B

2,6-dibromo-cyclopenta[def]phenanthren-4-one (1.0 g, 2.76 mmol) wasdissolved in dry ether (30 ml) and THF (10 ml), and phenyl magnesiumbromide (3.0M in ether) was added slowly thereto and then the resultantmixture was refluxed for 3 hours. By adding water to the mixture, thereaction was terminated. 1N—HCl solution was added to the mixture untilpH of the mixture to be 3-4 and the resultant was extracted with ethylacetate. The organic layer was dried over anhydrous sodium sulfate,filtered and concentrated under a reduced pressure. The obtained solidwas purified by silica gel column chromatography to give a desiredcompound (0.79 g, 65%).

2) Synthesis of Compound 5

The intermediate B (0.79 g, 1.79 mmol) was dissolved in dry benzene (20ml) and trifluoromethane sulfonic acid (0.48 ml, 5.38 mmol, 3 eq.) wasdropwise added thereto and then the mixture was stirred at 80° C. for 2hours. The resultant was diluted with water, extracted with ethylacetate. The organic layer was dried over anhydrous magnesium sulfate,filtered and concentrated to obtain a solid. The obtained solid waspurified by silica gel column chromatography to give a desired compound(0.65 g, 63%).

¹H NMR (300 MHz, CDCl₃, δ): 7.22-7.26(m, 10H), 7.70(s, 2H), 7.80(s, 3H),8.00(s, 2H)

3) Synthesis of Material 5 (Formula 15)

A material 5 represented by Formula 15 was synthesized in the samemanner as in the synthesis of the material 1 of Synthesis Example 1except that the compound 5 was used instead of the compound 2, and9H-carbazole was used instead of bis(4-biphenyl)amine.

¹H NMR (300 MHz, CDCl₃, δ): 8.02-6.89 (m, 32H).

4) Synthesis of Material 6 (Formula 27)

A material 6 represented by Formula 27 was synthesized in the samemanner as in the synthesis of the material 1 of Synthesis Example 1except that the compound 5 was used instead of the compound 2.

¹H NMR (300 MHz, CDCl3, δ): 8.05-7.75(6H, m), 7.55-6.68 (m, 36H).

5) Synthesis of Material 7(Formula 35)

4-bromo triphenylamine 7.6 g (23.45 mmol), aniline 21.85 g (0.235 mol),sodium tert-butoxide 6.76 g (70 mmol). Pd₂(dba)₃[(tris(dibenzilideneacetone)dipalladium(0))] 0.86 g (0.938 mmol) andtri(tert-butyl)phosphine 0.23 g (1.173 mmol) in 500 ml round bottomflask were dissolved with toluene 200 ml, and refluxed for 12 hours.After the reaction was terminated, the reaction solution was cooled toroom temperature, and 200 ml of distilled water was added thereto toextract an organic layer. The organic layer was dried over MgSO₄,concentrated, and purified by silica gel column chromatography. Theeluate was concentrated and dried to giveN,N,N′-triphenyl-p-phenylenediamine (6.71 g, 85%).

The obtained N,N,N′-triphenyl-p-phenylenediamine (3.36 g, 10.0 mmol),compound 5 (2.0 g, 4.0 mmol), sodium tert-butoxide (1.15 g, 12 mmol),Pd₂(dba)₃[(tris(dibenzylidene acetone)dipalladium(0))] (0.14 g, 0.16mmol) and tri(tert-butyl)phosphine (0.04 g, 0.2 mmol) in 100 ml roundbottom flask were dissolved with 50 ml of toluene and refluxed for 12hours. After the reaction was terminated, the reaction solution wascooled to room temperature and 50 ml of distilled water was addedthereto to extract an organic layer. The obtained organic layer wasdried over MgSO₄, concentrated, and purified by silica gel columnchromatography. The eluate was concentrated and dried to give material 7represented by Formula 35 (2.91 g, yield: 72%).

¹H NMR (300 MHz, CDCl₃, δ): 7.86-7.71(6H, m), 7.32-6.64(m, 48H).

Synthesis Example 5 1) Synthesis of Intermediate C

2,6-dibromo-cyclopenta[def]phenanthren-4-one (0.95 g, 2.62 mmol) andphenol (30 ml) were added to a 250 ml 3-neck round bottom flask. Thereaction mixture was heated and incubated for five hours while a HCl gaswas run into the mixture. After the reaction was terminated, thereaction solution was concentrated under a reduced pressure to removeunreacted phenol. The residue was purified by silica gel columnchromatography to give an intermediate C (0.59 g, 42%).

2) Synthesis of Compound 6

The intermediate C (0.95 g, 2.62 mmol) was placed in a 100 ml roundbottom flask, and DMF (5 ml) and acetonitrile (20 ml) were addedthereto. K₂CO₃ (1.52 g) and octyl bromide (2.11 g) were sequentiallyadded, and the reaction mixture was heated and refluxed for 18 hours.After the reaction was terminated, the organic layer was separated andpurified by silica gel column chromatography to give a compound 4 (0.68g, 82%).

¹H NMR (300 MHz, CDCl₃, δ): 7.78 (2H, d) 7.79(2H, s) 7.67 (2H, d)7.11(4H, dd) 3.89 (4H, t) 1.74 (4H, q) 1.28 (20H, m) 0.88 (6H, m)

4) Synthesis of Material 8 (Formula 38)

A material 8 represented by Formula 38 was synthesized in the samemanner as in the synthesis of the material 1 of Synthesis Example 1except that the compound 6 was used instead of the compound 2, and9H-carbazole was used instead of bis(4-biphenyl)amine.

¹H NMR (300 MHz, CDCl₃, δ): 7.85-6.92(30H, m) (4H, dd) 3.89 (4H, t) 1.74(4H, q) 1.28 (20H, m) 0.88 (6H, m)

5) Synthesis of Material 9 (Formula 39)

A material 9 represented by Formula 39 was synthesized in the samemanner as in the synthesis of the material 4 of Synthesis Example 3except that the compound 6 was used instead of the compound 4.

¹H NMR (300 MHz, CDCl₃, δ): 7.95-6.75(50H, m) (4H, dd) 3.89 (4H, t) 1.74(4H, q) 1.28 (20H, m) 0.88 (6H, m)

Evaluation Example Evaluation of Optical Characteristics of Materials1-5

The photoluminescence (PL) spectra of the materials in a solution phaseand a film phase were measured to evaluate the emission characteristicsof the materials.

In order to evaluate optical characteristics of a solution phase, eachof the materials 3, 4, 8 and 9 was diluted to a concentration of 10 mMwith toluene, and the PL spectra of the diluted solutions were measuredusing an ISC PC1 spectrofluorometer equipped with a xenon lamp. Also, inorder to evaluate optical characteristics of a film phase, quartzsubstrates were prepared and washed with acetone and pure water. Then,the materials 3, 4, 8 and 9 were spin-coated on the substrates andheated at 110° C. for 30 minutes to form films with a thickness of 1,000Å. The PL spectra of the films were measured. The results are presentedin Table 1 below. As shown in Table 1, it can be seen that the materialsaccording to the present invention have emission characteristicssuitable for organic EL devices.

TABLE 1 Material Solution (λ_(max))(nm) Film (λ_(max))(nm) 3 390 397 4420 445 8 395 398 9 420 450

Example 1

Organic EL devices having the following structure were manufacturedusing the material 1 as a hole transport layer, the compound of Formula47 as a hole injection layer, the compound of Formula 48 as host of thelight-emitting layer and the compound of Formula 49 as a dopant of thelight-emitting layer: ITO/Formula 47 (200 Å)/material 1 (300 Å)/Formula48: Formula 49 (300 Å)/Alq3 (40 Å)/LiF (10 Å)/Al (2000 Å).

A 15 Ω/cm² (1,000 Å) ITO glass substrate was cut into pieces of 50 mm×50mm×0.7 mm in size, followed by ultrasonic cleaning in acetone, isopropylalcohol, and pure water (15 minutes for each) and then UV/ozone cleaning(30 minutes) to form anodes. The compound of Formula 47 (hole injectionlayers) and the material 1 (hole transport layers) were vacuum depositedon the anodes. A mixture of the compound of Formula 48 and the compoundof Formula 49 (weight ratio of 100:5) was vacuum deposited to formlight-emitting layers. Then, an Alq3 compound was vacuum deposited to athickness of 40 Å on the light-emitting layers to form electrontransport layers. LiF (10 Å, electron injection layers) and Al (2000 Å,cathodes) were sequentially vacuum-deposited on the electron transportlayers to thereby complete organic EL devices as shown in FIG. 1A. Theorganic EL devices exhibited red emission of 14,000 cd/m² at a voltageof 6.0V and efficiency of 5.45 cd/A.

Example 2

Organic EL devices having the following structure were manufacturedusing the material 3 as a host of a light-emitting layer and thecompound of Formula 50 as a dopant of the light-emitting layer:ITO/Formula 47 (200 Å)/α-NPD(300 Å)/material 3: Formula 50 (300 Å)/Alq3(40 Å)/LiF (10 Å)/Al (2000 Å).

A 15Ω/cm² (1,000 Å) ITO glass substrate was cut into pieces of 50 mm×50mm×0.7 mm in size, followed by ultrasonic cleaning in acetone, isopropylalcohol, and pure water (15 minutes for each) and then UV/ozone cleaning(30 minutes) to form anodes. The compound of Formula 47 (hole injectionlayers) and α-NPD (hole transport layers) were vacuum deposited on theanodes. A mixture of the material 3 and RD15 (Formula 50) (weight ratioof 100:10) was vacuum deposited to form light-emitting layers. Then, anAlq3 compound was vacuum deposited to a thickness of 40 Å on thelight-emitting layers to form electron transport layers. LiF (10 Å,electron injection layers) and Al (2000 Å, cathodes) were sequentiallyvacuum-deposited on the electron transport layers to thereby completeorganic EL devices as shown in FIG. 1A. The organic EL devices exhibitedred emission of 1200 cd/m² at a voltage of 10V and efficiency of 4.32cd/A. The voltage-efficiency characteristics of the organic EL devicesare illustrated in FIG. 2A.

Example 3

Organic EL devices having the following structure were manufactured inthe same manner as in Example 1 except that α-NPD was used as a holetransport layer and the material 4 as a dopant of the light-emittinglayer: ITO/Formula 47 (200 Å)/α-NPD(300 Å)/Formula 48: material 4(300Å)/Alq3(40 Å)/LiF(10 Å)/Al(2000 Å). The organic EL devices exhibitedblue emission of 4600 cd/m² at a voltage of 8V and efficiency of 5.4cd/A.

Example 4

Organic EL devices having the following structure were manufactured inthe same manner as in Example 2 except that the material 5 was used as ahost of a light-emitting layer: ITO/Formula 47 (200 Å)/α-NPD(300Å)/material 5: Formula 50 (300 Å)/Alq3(40 Å)/LiF(10 Å)/Al(2000 Å). Theorganic EL devices exhibited blue emission of 6500 cd/m² at a voltage of10V and efficiency of 7.48 cd/A.

Example 5

Organic EL devices having the following structure were manufactured inthe same manner as in Example 1 except that the material 6 as a holetransport layer: ITO/Formula 47 (200 Å)/material 6(300 Å)/Formula 48:Formula 49 (300 Å)/Alq3(40 Å)/LiF(10 Å)/Al(2000 Å). The organic ELdevices exhibited blue emission of 15,800 cd/m² at a voltage of 6.5V andefficiency of 7.66 cd/A.

Example 6

Organic EL devices having the following structure were manufactured inthe same manner as in Example 1 except that the material 7 was used ashole injection layer and α-NPD as a hole transport layer: ITO/material 7(200 Å)/α-NPD(300 Å)/Formula 48: Formula 49(300 Å)/Alq3(40 Å)/LiF(10Å)/Al(2000 Å). The organic EL devices exhibited blue emission of 15,000cd/m² at a voltage of 6.0V and efficiency of 6.48 cd/A.

Example 7

Organic EL devices having the following structure were manufacturedusing the material 8 as a host of light-emitting layer and the compoundof Formula 50 as a dopant of light-emitting layer: ITO/PEDOT(400Å)/material 8: Formula 50 (300 Å)/Alq3(40 Å)/LiF(10 Å)/Al(2000 Å).

A 15Ω/cm² (1,000 Å) ITO glass substrate was out into pieces of 50 mm×50mm×0.7 mm in size, followed by ultrasonic cleaning in acetone, isopropylalcohol, and pure water (15 minutes for each) and then UV/ozone cleaning(30 minutes) to form anodes. PEDOT-PSS (Al4083) (Bayer) was coated onthe anodes and heated in air at 110° C. for 5 minutes and then in anitrogen atmosphere at 200° C. for 5 minutes to form hole injectionlayers with a thickness of 400 Å. A mixture of the material 8 (0.1 g) asa host and the compound of Formula 50 (0.01 g) as a dopant (10 parts byweight of the compound of Formula 50 based on 100 parts by weight of thematerial 8) was spin-coated on the hole injection layers and heated at100° C. for 30 minutes to form light-emitting layers with a thickness of300 Å. Then, an Alq3 compound was vacuum deposited to a thickness of 40Å on the light-emitting layers to form electron transport layers. LiF(10 Å, electron injection layers) and Al (2000 Å, cathodes) weresequentially vacuum-deposited on the electron transport layers tothereby complete organic EL devices as shown in FIG. 1B. The organic ELdevices exhibited red emission of 1500 cd/m² at a voltage of 9V andefficiency of 4.1 cd/A. The voltage-efficiency characteristics of theorganic EL devices are illustrated in FIG. 2B.

Example 8

Organic EL devices having the following structure were manufactured inthe same manner as in Example 7 except that the compound of Formula 48was used as a host of a light-emitting layer, and the material 9 as adopant of the light-emitting layer: ITO/PEDOT(400 Å)/Formula 48:material 9 (300 Å)/Alq3(40 Å)/LiF(10 Å)/Al (2000 Å). The organic ELdevices exhibited blue emission of 3700 cd/m² at a voltage of 6V andefficiency of 4.2 cd/A.

From the above Examples, it can be seen that the materials of thepresent invention have good EL characteristics as phosphorescent andfluorescent materials.

A compound of Formula 1 according to the present invention is availablefor both dry and wet processes, and has good emission characteristicsand thermal stability. Therefore, the use of the compound of the presentinvention enables to produce an organic EL device having a low drivingvoltage and good color purity and efficiency.

1. An organic electroluminescent (EL) device comprising: a firstelectrode; a second electrode; and at least one organic layer locatedbetween the first electrode and the second electrode, the organic layercomprising an organic compound represented by formula 1:

wherein Y and Q are the same or different and each is a substituted orunsubstituted C2-C30 alkylene group, a substituted or unsubstitutedC6-C30 cycloalkylene group, a substituted or unsubstituted C6-C30arylene group, a substituted or unsubstituted C2-C30 heteroarylenegroup, or a substituted or unsubstituted C2-C30 alkenylene group; m isan integer of 0 to 5; n is an integer of 0 to 5; R₁ and R₂, when linkedtogether, form one of rings represented by Formulae 2 through 5:

wherein “R₉”s are the same or different and each is a hydrogen, ahalogen, a cyano group, a hydroxyl group, a substituted or unsubstitutedC1-C20 alkyl group, a substituted or unsubstituted C3-C20 cycloalkylgroup, a substituted or unsubstituted C2-C30 heterocycloalkyl group, asubstituted or unsubstituted C1-C20 alkoxy group, a substituted orunsubstituted C6-C30 aryl group, a substituted or unsubstituted C6-C30aralkyl group, a substituted or unsubstituted C2-C30 heteroaryl group,—N(G₁)(G₂), or —Si(G₃)(G₄)(G₅) where G₁, G₂, G₃, G₄, and G₅ are eachindependently a hydrogen, a substituted or unsubstituted C1-C20 alkylgroup, a substituted or unsubstituted C6-C30 aryl group, a substitutedor unsubstituted C2-C30 heteroaryl group, a substituted or unsubstitutedC5-C20 cycloalkyl group, or a substituted or unsubstituted C2-C30heterocycloalkyl group; and A is a single bond, —O—, —S—, —(CH₂)_(s)—,where s is an integer of 1 to 5; R₃, R₄, R₅, R₆, R₇, and R₈ are the sameor different and each is a hydrogen, a halogen, a cyano group, ahydroxyl group, a substituted or unsubstituted C1-C20 alkyl group, asubstituted or unsubstituted C3-C20 cycloalkyl group, a substituted orunsubstituted C2-C30 heterocycloalkyl group, a substituted orunsubstituted C1-C20 alkoxy group, a substituted or unsubstituted C6-C30aryl group, a substituted or unsubstituted C6-C30 aralkyl group, asubstituted or unsubstituted C2-C30 heteroaryl group, —N(G₁)(G₂), or—Si(G₃)(G₄)(G₅) where G₁, G₂, G₃, G₄, and G₅ are each independently ahydrogen, a substituted or unsubstituted C1-C20 alkyl group, asubstituted or unsubstituted C6-C30 aryl group, a substituted orunsubstituted C2-C30 heteroaryl group, a substituted or unsubstitutedC5-C20 cycloalkyl group, or a substituted or unsubstituted C2-C30heterocycloalkyl group; Z₁, Z₂, Z₃, and Z₄ are the same or different andeach is a substituted or unsubstituted C1-C20 alkyl group, a substitutedor unsubstituted C3-C20 cycloalkyl group, a substituted or unsubstitutedC2-C30 heterocycloalkyl group, a substituted or unsubstituted C1-C20alkoxy group, a substituted or unsubstituted C6-C30 aryl group, asubstituted or unsubstituted C2-C30 heteroaryl group, a substituted orunsubstituted C6-C30 aralkyl group, a substituted or unsubstitutedC8-C30 allylaryl group, a substituted or unsubstituted C1-C20 alkylenegroup, a substituted or unsubstituted C6-C30 arylene group, or asubstituted or unsubstituted C2-C30 heteroarylene group; X is a singlebond, —CH═CH—, —O—, —S—, —Se—, or —C(R′R″)— where R′ and R″ are the sameas R₃, or —(CH₂)_(p)— where p is an integer of 1 to 10; and o is 0 or 1.2. The organic EL device of claim 1, wherein the organic layer is alight-emitting layer, a hole injection layer, or a hole transport layer.3. The organic EL device of claim 1, wherein the organic EL devicefurther comprising at least one selected from the group consisting of ahole injection layer, a hole transport layer, an electron blockinglayer, a hole blocking layer, an electron transport layer, and anelectron injection layer, between the first electrode and the secondelectrode.
 4. An organic electroluminescent (EL) device, comprising: afirst electrode; a second electrode; and an organic layer comprising anemissive layer between the first electrode and the second electrode, theorganic layer comprising an organic compound represented by Formula 1:

wherein Y and Q are the same or different and each is a substituted orunsubstituted C2-C30 alkylene group, a substituted or unsubstitutedC6-C30 cycloalkylene group, a substituted or unsubstituted C6-C30arylene group, a substituted or unsubstituted C2-C30 heteroarylenegroup, or a substituted or unsubstituted C2-C30 alkenylene group; m isan integer of 0 to 5; n is an integer of 0 to 5; R₁ and R₂ are the sameor different and each is a hydrogen, a halogen, a cyano group, ahydroxyl group, a substituted or unsubstituted C1-C20 alkyl group, asubstituted or unsubstituted C3-C20 cycloalkyl group, a substituted orunsubsututed C2-C30 heterocycloalkyl group, a substituted orunsubstituted C1-C20 alkoxy group, a substituted or unsubstituted C6-C30aryl group, a substituted or unsubstituted C6-C30 aralkyl group, asubstituted or unsubstituted C2-C30 heteroaryl group, R₁ and R₂ may belinked together, and R₁ and R₂, when linked together, form a substitutedor unsubstituted C3-C20 aliphatic ring, a substituted or unsubstitutedC5-C30 heteroaliphatic ring, a substituted or unsubstituted C6-C30aromatic ring, or a substituted or unsubstituted C2-C30 heteroaromaticring; R₃, R₄, R₅, R₆, R₇, and R₈ are the same or different and each is ahydrogen, a halogen, a cyano group, a hydroxyl group, a substituted orunsubstituted C1-C20 alkyl group, a substituted or unsubstituted C3-C20cycloalkyl group, a substituted or unsubstituted C2-C30 heterocycloalkylgroup, a substituted or unsubstituted C1-C20 alkoxy group, a substitutedor unsubstituted C6-C30 aryl group, a substituted or unsubstitutedC6-C30 aralkyl group, a substituted or unsubstituted C2-C30 heteroarylgroup, —N(G₁)(G₂), or —Si(G₃)(G₄)(G₅) where G₁, G₂, G₃, G₄, and G₅ areeach independently a hydrogen, a substituted or unsubstituted C1-C20alkyl group, a substituted or unsubstituted C6-C30 aryl group, asubstituted or unsubstituted C2-C30 heteroaryl group, a substituted orunsubstituted C5-C20 cycloalkyl group, or a substituted or unsubstitutedC2-C30 heterocycloalkyl group; Z₁, Z₂, Z₃, and Z₄ are the same ordifferent and each is a substituted or unsubstituted C1-C20 alkyl group,a substituted or unsubstituted C3-C20 cycloalkyl group, a substituted orunsubstituted C2-C30 heterocycloalkyl group, a substituted orunsubstituted C1-C20 alkoxy group, a substituted or unsubstituted C6-C30aryl group, a substituted or unsubstituted C2-C30 heteroaryl group, asubstituted or unsubstituted C6-C30 aralkyl group, a substituted orunsubstituted C8-C30 allylaryl group, a substituted or unsubstitutedC1-C20 alkylene group, a substituted or unsubstituted C6-C30 arylenegroup, or a substituted or unsubstituted C2-C30 heteroarylene group; Xis a single bond, —CH═CH—, —O—, —S—, —Se—, or —C(R′R″)— where R′ and R″are the same as R₃, or —(CH₂)_(p)— where p is an integer of 1 to 10; ando is 0or
 1. 5. The organic EL device of claim 4, wherein the organiclayer is the emissive layer.
 6. The organic EL device of claim 4,wherein the organic layer further comprises a hole injection layerlocated between the first electrode and the emissive layer, and at leastone of the emissive layer and the hole injection layer comprises theorganic compound represented by Formula
 1. 7. The organic EL device ofclaim 6, wherein the hole injection layer comprises the organic compoundrepresented by Formula
 1. 8. The organic EL device of claim 4, whereinthe organic layer further comprises a hole injection layer locatedbetween the first electrode and the emissive layer, and a hole transportlayer located between the hole injection layer and the emissive layer,and at least one of the emissive layer, the hole injection layer and thehole transport layer comprises the organic compound represented byFormula
 1. 9. The organic EL device of claim 8, wherein the holetransport layer comprises the organic compound represented by Formula 1.10. The organic EL device of claim 4, wherein in Formula 1, R₁ and R₂,when linked together, form one of rings represented by Formulae 2through 5:

wherein “R₉”s are the same or different and each is a hydrogen, ahalogen, a cyano group, a hydroxyl group, a substituted or unsubstitutedC1-C20 alkyl group, a substituted or unsubstituted C3-C20 cycloalkylgroup, a substituted or unsubstituted C2-C30 heterocycloalkyl group, asubstituted or unsubstituted C1-C20 alkoxy group, a substituted orunsubstituted C6-C30 aryl group, a substituted or unsubstituted C6-C30aralkyl group, a substituted or unsubstituted C2-C30 heteroaryl group,—N(G₁)(G₂), or —Si(G₃)(G₄)(G₅) where G₁, G₂, G₃, G₄, and G₅ are eachindependently a hydrogen, a substituted or unsubstituted C1-C20 alkylgroup, a substituted or unsubstituted C6-C30 aryl group, a substitutedor unsubstituted C2-C30 heteroaryl group, a substituted or unsubstitutedC5-C20 cycloalkyl group, or a substituted or unsubstituted C2-C30heterocycloalkyl group; and A is a single bond, —O—, —S—, —(CH₂)_(s)—,where s is an integer of 1 to
 5. 11. The organic EL device of claim 4,wherein the organic compound is one of the compounds represented byFormulae 6 through 8:

wherein Y and Q are the same or different and each is a substituted orunsubstituted C2-C30 alkylene group, a substituted or unsubstitutedC6-C30 cycloalkylene group, a substituted or unsubstituted C6-C30arylene group, a substituted or unsubstituted C2-C30 heteroarylenegroup, or a substituted or unsubstituted C2-C30 alkenylene group; m isan integer of 0 to 5; n is an integer of 0 to 5; R₁′ and R₂′ are thesame or different and each is a hydrogen, a halogen, a cyano group, ahydroxyl group, a substituted or unsubstituted C1-C20 alkyl group, asubstituted or unsubstituted C3-C20 cycloalkyl group, a substituted orunsubstituted C2-C30 heterocycloalkyl group, a substituted orunsubstituted C1-C20 alkoxy group, a substituted or unsubstituted C6-C30aryl group, a substituted or unsubstituted C6-C30 aralkyl group, asubstituted or unsubstituted C2-C30 heteroaryl group; Z₁, Z₂, Z₃, and Z₄are the same or different and each is a substituted or unsubstitutedC1-C20 alkyl group, a substituted or unsubstituted C3-C20 cycloalkylgroup, a substituted or unsubstituted C2-C30 heterocycloalkyl group, asubstituted or unsubstituted C1-C20 alkoxy group, a substituted orunsubstituted C6-C30 aryl group, a substituted or unsubstituted C2-C30heteroaryl group, a substituted or unsubstituted C6-C30 aralkyl group, asubstituted or unsubstituted C2-C30 allylaryl group, a substituted orunsubstituted C1-C20 alkylene group, a substituted or unsubstitutedC6-C30 arylene group, or a substituted or unsubstituted C2-C30heteroarylene group; X is a single bond, —CH═CH—, —O—, —S—, —Se—, or—C(R′, R″)— where R′ and R″ are the same as R₃, or —(CH₂)_(p)— where pis an integer of 1 to 10; o is 0 or 1; and “R₁₀”s are the same ordifferent and each is a hydrogen, a halogen, a cyano group, a hydroxylgroup, a substituted or unsubstituted C1-C20 alkyl group, a substitutedor unsubstituted C3-C20 cycloalkyl group, a substituted or unsubstitutedC2-C30 heterocycloalkyl group, a substituted or unsubstituted C1-C20alkoxy group, a substituted or unsubstituted C6-C30 aryl group, asubstituted or unsubstituted C6-C30 aralkyl group, a substituted orunsubstituted C2-C30 heteroaryl group, —N(G₁)(G₂), or —Si(G₃)(G₄)(G₅)where G₁, G₂, G₃, G₄, and G₅ are each independently a hydrogen, asubstituted or unsubstituted C1-C20 alkyl group, a substituted orunsubstituted C6-C30 aryl group, a substituted or unsubstituted C2-C30heteroaryl group, a substituted or unsubstituted C5-C20 cycloalkylgroup, or a substituted or unsubstituted C2-C30 heterocycloalkyl group.12. The organic EL device of claim 4, wherein the organic compound isone of the compounds represented by Formulae 9 through 46:


13. An organic electroluminescent (EL) device, comprising: a firstelectrode; a second electrode; an emissive layer located between thefirst electrode and the second electrode; a hole injection layer locatedbetween the first electrode and the emissive layer; a hole transportlayer located between the hole injection layer and the emissive layer,at least one of the emissive layer, the hole injection layer and thehole transport layer is an organic layer comprising an organic compoundselected from the group consisting of compounds represented by Formulae6 through 8:

wherein Y and Q are the same or different and each is a substituted orunsubstituted C2-C30 alkylene group, a substituted or unsubstitutedC6-C30 cycloalkylene group, a substituted or unsubstituted C6-C30arylene group, a substituted or unsubstituted C2-C30 heteroarylenegroup, or a substituted or unsubstituted C2-C30 alkenylene group; m isan integer of 0 to 5; n is an integer of 0 to 5; R₁′ and R₂′ are thesame or different and each is a hydrogen, a halogen, a cyano group, ahydroxyl group, a substituted or unsubstituted C1-C20 alkyl group, asubstituted or unsubstituted C3-C20 cycloalkyl group, a substituted orunsubstituted C2-C30 heterocycloalkyl group, a substituted orunsubstituted C1-C20 alkoxy group, a substituted or unsubstituted C6-C30aryl group, a substituted or unsubstituted C6-C30 aralkyl group, asubstituted or unsubstituted C2-C30 heteroaryl group; Z₁, Z₂, Z₃, and Z₄are the same or different and each is a substituted or unsubstitutedC1-C20 alkyl group, a substituted or unsubstituted C3-C20 cycloalkylgroup, a substituted or unsubstituted C2-C30 heterocycloalkyl group, asubstituted or unsubstituted C1-20 alkoxy group, a substituted orunsubstituted C6-C30 aryl group, a substituted or unsubstituted C2-C30heteroaryl group, a substituted or unsubstituted C6-C30 aralkyl group, asubstituted or unsubstituted C2-C30 allylaryl group, a substituted orunsubstituted C1-C20 alkylene group, a substituted or unsubstitutedC6-C30 arylene group, or a substituted or unsubstituted C2-C30heteroarylene group; X is a single bond, —CH═CH—, —O—, —S—, —Se—, or—C(R′, R″)— where R′ and R″ are the same as R₃, or —(CH₂)_(p)— where pis an integer of 1 to 10; o is 0 or 1; and “R₁₀”s are the same ordifferent and each is a hydrogen, a halogen, a cyano group, a hydroxylgroup, a substituted or unsubstituted C1-C20 alkyl group, a substitutedor unsubstituted C3-C20 cycloalkyl group, a substituted or unsubstitutedC2-C30 heterocycloalkyl group, a substituted or unsubstituted C1-C20alkoxy group, a substituted or unsubstituted C6-C30 aryl group, asubstituted or unsubstituted C6-C30 aralkyl group, a substituted orunsubstituted C2-C30 heteroaryl group, —N(G₁)(G₂), or —Si(G₃)(G₄)(G₅)where G₁, G₂, G₃, G₄, and G₅ are each independently a hydrogen, asubstituted or unsubstituted C1-C20 alkyl group, a substituted orunsubstituted C6-C30 aryl group, a substituted or unsubstituted C2-C30heteroaryl group, a substituted or unsubstituted C5-C20 cycloalkylgroup, or a substituted or unsubstituted C2-C30 heterocycloalkyl group.14. The organic El device of claim 13, wherein the organic layer is theemissive layer.
 15. The organic EL device of claim 13, wherein theorganic layer is the hole injection layer.
 16. The organic EL device ofclaim 13, wherein the organic layer is the hole transport layer.